| Literature DB >> 33668373 |
Sergey N Podyachev1, Rustem R Zairov1, Asiya R Mustafina1.
Abstract
The present review is aimed at highlighting outlooks for cyclophanic 1,3-diketones as a new type of versatile ligands and building blocks of the nanomaterial for sensing and bioimaging. Thus, the main synthetic routes for achieving the structural diversity of cyclophanic 1,3-diketones are discussed. The structural diversity is demonstrated by variation of both cyclophanic backbones (calix[4]arene, calix[4]resorcinarene and thiacalix[4]arene) and embedding of different substituents onto lower or upper macrocyclic rims. The structural features of the cyclophanic 1,3-diketones are correlated with their ability to form lanthanide complexes exhibiting both lanthanide-centered luminescence and magnetic relaxivity parameters convenient for contrast effect in magnetic resonance imaging (MRI). The revealed structure-property relationships and the applicability of facile one-pot transformation of the complexes to hydrophilic nanoparticles demonstrates the advantages of 1,3-diketone calix[4]arene ligands and their complexes in developing of nanomaterials for sensing and bioimaging.Entities:
Keywords: 1,3-diketone; calixarenes; complexation; lanthanides; ligands; luminescence; macrocycles; nanoparticle; supramolecular chemistry
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Year: 2021 PMID: 33668373 PMCID: PMC7956255 DOI: 10.3390/molecules26051214
Source DB: PubMed Journal: Molecules ISSN: 1420-3049 Impact factor: 4.411